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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 879769생성일: 2026년 10월 25일

(S)-Methyl 3-([1,1'-biphenyl]-4-yl)-2-aminopropanoate → (s)-3-Biphenyl-4-yl-2-({(s)-3-[4-(3,4-dichloro-benzyloxy)-phenyl]-2,3,6,7,8,9-hexahydro-[1,4]dioxino-[2,3-g]isoquinoline-8-carbonyl}-amino)-propionic acid methyl ester hydrochloride salt

https://huagongshe.com/reaction/879769

반응식

참여 물질

역할이름HCID투입량
반응물(S)-Methyl 3-([1,1'-biphenyl]-4-yl)-2-aminopropanoateHCID 15714801—
반응물(S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-2,3,8,9-tetrahydro-6H-[1,4]dioxino[2,3-g]isoquinoline-7,8-dicarboxylic acid 7-tert-butyl esterHCID 66719307—
생성물(s)-3-Biphenyl-4-yl-2-({(s)-3-[4-(3,4-dichloro-benzyloxy)-phenyl]-2,3,6,7,8,9-hexahydro-[1,4]dioxino-[2,3-g]isoquinoline-8-carbonyl}-amino)-propionic acid methyl ester hydrochloride saltHCID 66719550112.5%

반응 단계

(S)-3-[4-(3,4-Dichloro-benzyloxy)-phenyl]-2,3,8,9-tetrahydro-6H-[1,4]dioxino[2,3-g]isoquinoline-7,8-dicarboxylic acid 7-tert-butyl ester (59 mg) was coupled with (S)-2-amino-3-biphenyl-4-yl-propionic acid methyl ester (31 mg) according to General Procedure A. The resulting Boc-protected amine was treated as described in General Procedure C to give (S)-3-Biphenyl-4-yl-2-({(S)-3-[4-(3,4-dichloro-benzyloxy)-phenyl]-2,3,6,7,8,9-hexahydro-[1,4]dioxino-[2,3-g]isoquinoline-8-carbonyl}-amino)-propionic acid methyl ester hydrochloride salt (43 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987295B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-19b339f44ff84ab5afc5d3d7cb2cbfb6
출처 메모uspto-grants-2015_03